EP0721962A2 - Gummi-modifiziertes, thermoplastisches Harz und dieses enthaltende Zusammensetzung - Google Patents

Gummi-modifiziertes, thermoplastisches Harz und dieses enthaltende Zusammensetzung Download PDF

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Publication number
EP0721962A2
EP0721962A2 EP96300026A EP96300026A EP0721962A2 EP 0721962 A2 EP0721962 A2 EP 0721962A2 EP 96300026 A EP96300026 A EP 96300026A EP 96300026 A EP96300026 A EP 96300026A EP 0721962 A2 EP0721962 A2 EP 0721962A2
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EP
European Patent Office
Prior art keywords
thermoplastic resin
rubber
weight
modified thermoplastic
component
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP96300026A
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English (en)
French (fr)
Other versions
EP0721962B1 (de
EP0721962A3 (de
Inventor
Hajime Miyajima
Tsugio Asakawa
Noriaki Ijuin
Hiroo Nakamura
Toshihiro Ogawa
Shinichi Kimura
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
JSR Corp
Original Assignee
Japan Synthetic Rubber Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from JP02093495A external-priority patent/JP3216466B2/ja
Priority claimed from JP14821995A external-priority patent/JP3235411B2/ja
Application filed by Japan Synthetic Rubber Co Ltd filed Critical Japan Synthetic Rubber Co Ltd
Publication of EP0721962A2 publication Critical patent/EP0721962A2/de
Publication of EP0721962A3 publication Critical patent/EP0721962A3/de
Application granted granted Critical
Publication of EP0721962B1 publication Critical patent/EP0721962B1/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F279/00—Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00
    • C08F279/02—Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00 on to polymers of conjugated dienes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L51/04—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to rubbers

Definitions

  • This invention relates to a rubber-modified thermoplastic resin which is suitable for being blended with another thermoplastic resin to impart, to the latter, an excellent mechanical strength such as tensile strength, flexural strength or the like and an excellent impact resistance and to a composition comprising the above rubber-modified thermoplastic resin and another thermoplastic resin.
  • ABS resins Well-known rubber-modified thermoplastic resins include ABS resins and AES resins and these have been used in a large amount in industry.
  • the following two methods for producing the ABS resin have generally been known:
  • the above method (2) can produce with a good productivity many kinds of ABS resins having different qualities by appropriately selecting the amount of the rubber-rich ABS resin blended and appropriately selecting the kind of the AS resin.
  • the rubber-rich ABS resin is sometime used in the form of a blend with other thermoplastic resins than the AS resin; and when the rubber content of the rubber-rich ABS resin is increased, the same problem as mentioned above is caused with the said blend.
  • the present inventors have made extensive research on a solution of the above-mentioned problems encountered by the rubber-rich ABS resin having a rubber content of 50 to 85% by weight and have consequently found that the above problems can be solved by modifying the rubber-rich ABS resin having a rubber content of 50 to 85% by weight so that the Q value of the rubber-rich ABS resin becomes 30 x 10 -4 to 50 x 10 -3 cc/sec. It has been further found that when the rubber-rich ABS resin is modified so that the storage elastic modulus of the ace-tone-insoluble matter of the rubber-rich ABS resin falls within the specific range, the above-mentioned problems can be more satisfactorily solved.
  • An object of this invention is to provide a rubber-rich ABS resin having an increased rubber content by which the above-mentioned prior art problem has been solved.
  • Another object of this invention is to provide a thermoplastic resin composition comprising the above mentioned rubber-rich ABS resin with another thermoplastic resin.
  • a rubber-modified thermoplastic resin which is obtained by polymerizing (b) an aromatic vinyl compound and (c) a vinyl cyanide compound in the presence of (a) a rubbery polymer and in which the content of the component (a) is 50 to 85% by weight, the content of the component (b) is 5 to 48% by weight and the content of the component (c) is 2 to 45% by weight, and which resin has a Q value as defined herein of 30 x 10 -4 to 50 x 10 -3 cc/sec and a grafting degree of at least 5% by weight, preferably the acetone-insoluble matter of the rubber-modified thermoplastic resin having a storage elastic modulus of 5 x 10 7 to 1 x 10 9 Pa.
  • thermoplastic resin composition which comprises (A) the above-mentioned rubber-modified thermoplastic resin and (B) at least one other thermoplastic resin, the content of the component (a) in the composition being 3 to 35% by weight.
  • the rubber-modified thermoplastic resin (A) of this invention is obtained by polymerizing (b) an aromatic vinyl compound and (c) a vinyl cyanide compound in the presence of (a) a rubbery polymer, and in the rubber-modified thermoplastic resin (A), the content of the component (a) is 50 to 85% by weight; the content of the component (b) is 5 to 48% by weight; the content of the component (c) is 2 to 45% by weight; the Q value is 30 x 10 -4 to 50 x 10 -3 cc/sec; and the grafting degree is at least 5% by weight. It is preferable that the storage elastic modulus of the acetone-insoluble matter of the rubber-modified thermoplastic resin (A) is 5 x 10 7 to 1 x 10 9 Pa.
  • the rubbery polymer used as the component (a) in this invention includes, for example, polybutadiene, polyisoprene, styrene-butadiene copolymer (preferably having a styrene content of 5 to 60% by weight), styrene-isoprene copolymer, acrylonitrile-butadiene copolymer, ethylene- ⁇ -olefin copolymer, ethylene- ⁇ -olefin-polyene copolymer, acrylic rubber, butadiene-(meth)acrylic acid ester copolymer, styrene-butadiene block copolymer, styrene-isoprene block copolymer, hydrogenated styrene-butadiene block copolymer, hydrogenated butadiene polymer, ethylenic ionomer and the like.
  • the styrene-butadiene block copolymer and styrene-isoprene block copolymer include those having a structure of the AB type, the ABA type, the taper type and the radial teleblock type.
  • the hydrogenated butadiene polymer includes not only hydrogenation products of the above block copolymers but also hydrogenation products of block copolymers consisting of polystyrene block and styrene-butadiene random copolymer block, hydrogenation products of polymers consisting of polybutadiene block having a 1,2-vinyl content of 20% by weight or less and polybutadiene block having a 1,2-vinyl content of more than 20% by weight, etc. These rubbery polymers are used alone or in admixture of two or more.
  • the component (a) is preferably at least one conjugated diene rubber selected from the group consisting of polybutadiene and styrene-butadiene copolymer (preferably having a styrene content of 5 to 60% by weight), more preferably a mixture of the polybutadiene with the styrene-butadiene copolymer (the weight ratio of the former to the latter is 50-99/1-50).
  • the aromatic vinyl compound used as the component (b) includes, for example, styrene, t-butylstyrene, ⁇ -methylstyrene, p-methylstyrene, divinylbenzene, 1,1-diphenylstyrene, N,N-diethyl-p-aminoethylstyrene, N,N-diethyl-p-aminomethylstyrene, vinylpyridine, vinylxylene, monochlorostyrene, dichlorostyrene, monobromostyrene, fluorostyrene, ethylstyrene, vinylnaphthalene and the like. In particular, styrene and ⁇ -methylstyrene are preferable. These aromatic vinyl compounds are used alone or in admixture of two or more.
  • the vinyl cyanide compound used as the component (c) includes, for example, acrylonitrile and methacrylonitrile.
  • (d) other monomers can be used as far as they do not adversely affect the invention.
  • Said other monomers (d) include, for example, acrylic acid esters such as methyl acrylate, ethyl acrylate, propyl acrylate, butyl acrylate, amyl acrylate, hexyl acrylate, octyl acrylate, 2-ethylhexyl acrylate, cyclohexyl acrylate, dodecyl acrylate, octadecyl acrylate, phenyl acrylate, benzyl acrylate and the like; methacrylic acid esters such as methyl methacrylate, ethyl methacrylate, propyl methacrylate, butyl methacrylate, amyl methacrylate, hexyl methacrylate, octyl methacrylate, 2-ethylhexyl methacrylate, cyclo
  • the content of said other monomers (d) in the component (A) is preferably 20% by weight or less, more preferably 10% by weight or less, based on the total weight of the components other than the component (a).
  • the content of the component (a) in the rubber-modified thermoplastic resin (A) is 50 to 85% by weight, preferably 52 to 80% by weight, more preferably 54 to 78% by weight, and most preferably 55 to 75% by weight.
  • the content of the component (a) is less than 50% by weight, the productivity-improving effect is not sufficient, while when the content of the component (a) is more than 85% by weight, many fish eyes are formed and the appearance, impact resistance and mechanical strength are deteriorated.
  • the content of the component (b) in the rubber-modified thermoplastic resin (A) is 5 to 48% by weight, preferably 5 to 46% by weight, more preferably 10 to 45% by weight and most preferably 15 to 40% by weight.
  • the content of the component (c) is 2 to 45% by weight, preferably 2 to 43% by weight, more preferably 3 to 30% by weight and most preferably 4 to 25% by weight.
  • the content of the component (b) is less than 2% by weight
  • the content of the component (b) is more than 48% by weight
  • the content of the component (c) is less than 2% by weight
  • the content of the component (c) is more than 45% by weight
  • the weight ratio of the component (b) to the component (c) in the rubber-modified thermoplastic resin (A) is preferably 30-97/70-3, more preferably 40-95/60-5, more preferably 50-93/50-7 and most preferably 60-90/40-10.
  • the Q value of the rubber-modified thermoplastic resin (A) is 30 x 10 -4 to 50 x 10 -3 cc/sec, preferably 50 x 10 -4 to 40 x 10 -3 cc/sec, more preferably 60 x 10 -4 to 40 x 10 -3 cc/sec and most preferably 70 x 10 -4 to 35 x 10 -3 cc/sec.
  • the conditions for measuring the Q value are as follows:
  • the grafting degree of the rubber-modified thermoplastic resin (A) is at least 5% by weight, preferably 10 to 100% by weight and more preferably 12 to 80% by weight. When the grafting degree is less than 5% by weight, many fish eyes are formed and the appearance and impact resistance become inferior.
  • the grafting degree is herein defined as being the proportion of the copolymer component directly graft-bonded to the rubbery polymer to the amount of the rubber in the rubber-modified thermoplastic resin and can be controlled by varying the amount of a polymerization initiator, the polymerization temperature and the like.
  • the storage elastic modulus of the acetone-insoluble matter of the rubber-modified thermoplastic resin (A) is preferably 5 x 10 7 to 1 x 10 9 Pa, more preferably 7 x 10 7 to 8 x 10 8 Pa, most preferably 8 x 10 7 to 5 x 10 8 Pa and particularly preferably 1 x 10 8 to 4 x 10 8 Pa.
  • the storage elastic modulus is at least 5 x 10 7 Pa, the mechanical strength is excellent but when the storage elastic modulus exceeds 1 x 10 9 Pa, the impact resistance becomes insufficient.
  • the conditions for measuring the storage elastic modulus are as follows:
  • the contents of the components (a), (b) and (c) in the rubber-modified thermoplastic resin (A) can be appropriately controlled by varying the amounts of these components charged in the polymerization of them. Also, the contents of the components (a), (b) and (c) in the rubber-modified thermoplastic resin (A) can be determined from the amounts of these components charged, the polymerization conversions and the like. The contents can also be determined even by a known quantitative analysis method.
  • the control of the Q value and storage elastic modulus of the rubber-modified thermoplastic resin (A) can be effected by appropriately selecting the kinds and amounts of the chain transfer agent, the initiator and the like, appropriately selecting the polymerization temperature, or appropriately selecting the gel content or molecular weight of the rubbery polymer which is the component (a).
  • the method for producing the rubber-modified thermoplastic resin (A) includes a solution polymerization method, a bulk polymerization method, a suspension polymerization method, an emulsion polymerization method and a combination thereof.
  • the emulsion polymerization method is preferred, and in this emulsion polymerization method, a generally known polymerization adjuvant can be used.
  • the polymerization initiator used in the production of the rubber-modified thermoplastic resin (A) of this invention includes various organic peroxides such as hydroperoxides, alkyl peresters, percarbonates and the like, and preferable are cumene hydroperoxide, diisopropylbenzene hydroperoxide and t-butyl peroxyisopropyl carbonate.
  • organic peroxides such as hydroperoxides, alkyl peresters, percarbonates and the like
  • cumene hydroperoxide diisopropylbenzene hydroperoxide
  • t-butyl peroxyisopropyl carbonate t-butyl peroxyisopropyl carbonate
  • the amount of the above initiator used is preferably 0.1 to 2 parts by weight per 100 parts by weight of a total weight of the rubber components and the monomer components.
  • the chain transfer agent includes, for example, halogenated hydrocarbons (for example, chloroform, bromoform and the like), mercaptans (for example, n-dodecylmercaptan, t-dodecylmercaptan, n-octylmercaptan, n-hexadecylmercaptan and the like), terpenes (for example, dipentene, terpinolene and the like) and ⁇ -methylstyrene dimer.
  • halogenated hydrocarbons for example, chloroform, bromoform and the like
  • mercaptans for example, n-dodecylmercaptan, t-dodecylmercaptan, n-octylmercaptan, n-hexadecylmercaptan and the like
  • terpenes for example, dipentene, terpinolene and the like
  • the intrinsic viscosity of the methyl ethyl ketone-soluble matter of the rubber-modified thermoplastic resin which is the component (A) is preferably 0.15 to 1.5 dl/g, more preferably 0.2 to 1.2 dl/g, most preferably 0.25 to 1 dl/g and particularly preferably 0.3 to 0.8 dl/g, as measured in methyl ethyl ketone at 30°C
  • the at least one other thermoplastic resin (B) to be mixed with the rubber-modified thermoplastic resin (A) in this invention includes, for example, styrene resins such as ABS resin having a rubbery polymer content of less than 50% by weight, AES resin having a rubbery polymer content of less than 50% by weight, AAS resin having a rubbery polymer content of less than 50% by weight, AS resin, HIPS, PS and the like; olefin resins such as polyethylene, polypropylene and the like; polyamide resins such as PA6, PA66, PA46, PA12 and the like; polyester resins such as polybutylene terephthalate, polyethylene terephthalate, polyarylate and the like; polycarbonate resins; polyphenylene ether resins such as polyphenylene ether, polyphenylene ether/styrene resins and the like; polyacetal; vinyl chloride resin; polysulfone; polyphenylene sulfide (PPS); polyethersulfone;
  • thermoplastic resin (B) is preferably the following a. and b. which are used alone or in combination of two or more:
  • the above rubber-modified thermoplastic resins a include, for example, ABS resins, AES resins, AAS resins, MBS resins and the like, among which ABS resins and AES resins are preferable.
  • copolymers b. include the following copolymers:
  • an unsaturated acid anhydride monomer is used to obtain a copolymer and this copolymer is imidized.
  • the thus obtained post-imidized type copolymer is also included in the copolymers (iii).
  • aromatic vinyl compounds, vinyl cyanide compounds, (meth)acrylic acid esters and maleimide monomers used here include those mentioned above.
  • each component of the thermoplastic resin composition comprising (A) the rubber-modified thermoplastic resin and (B) at least one other thermoplastic resin
  • these components (A) and (B) are blended so that the rubbery polymer which is the component (a) of the rubber-modified thermoplastic resin (A) may be contained, preferably in a proportion of 3 to 35% by weight, in the composition.
  • the component (a) may be contained most preferably in a proportion of 5 to 25% by weight.
  • the content of the component (a) is less than 3% by weight, a sufficient impact strength is not obtained.
  • the content of the component (a) is more than 35% by weight, the molded article obtained therefrom becomes soft, which is not desirable.
  • the weight ratio of the component (A) to the component (B) is preferably 5-99/95-1, more preferably 7-95/93-5 and most preferably 10-90/90-10.
  • the rubber-modified thermoplastic resins (C) which are other than the rubber-modified thermoplastic resin (A) of this invention are used as the thermoplastic resin (B)
  • the rubbery polymer [referred to hereinafter as the component (a')] contained in the rubber-modified thermoplastic resin (C) is handled as follows:
  • the component (a') is also regarded as the component (a) and must satisfy the following conditions:
  • the total content of the components (a) and (a') is 3 to 35% by weight and the content of the component (a) is 3 to 35% by weight.
  • the content of the components (a) and (a') is 5 to 25% by weight and the content of the component (a) is 5 to 25% by weight.
  • thermoplastic resin composition of this invention can be prepared by kneading the rubber-modified thermoplastic resin (A) and at least one other thermoplastic resin (B) with, if necessary, various additives.
  • the kneading method includes methods using an extruder, a twin-roll mill, a Banbury mixer, a kneader and the like.
  • the kneading method is a method using an extruder, and the extruder includes a single screw extruder, a twin-screw extruder and the like.
  • all the components may be kneaded together, or a part of the components may be first kneaded followed by adding and kneading the remaining components in one portion or portions.
  • various additives may be added to the rubber-modified thermoplastic resin (A). If kneading is required in this case, the kneading may be effected by the above-mentioned method.
  • the above various additives include known coloring agents, pigments, lubricants, weathering agents, antistatic agents, antioxidants, flame retardants, heatage resistors, plasticizers, antibacterial agents, antifungal agents and the like.
  • thermoplastic resin composition of this invention can be molded into various molded articles by injection molding, sheet-extrusion molding, vacuum-forming, profile-extrusion molding, injection press molding, expansion molding, blow molding, injection blow molding or the like.
  • the rubber-modified thermoplastic resin (A) of this invention even when has a high rubber component content, can be blended with at least one other thermoplastic resin (B), and the molded articles obtained from the resulting blend are excellent in gloss, impact resistance and mechanical strength and greatly improved so that such an undesirable phenomenon that fish eyes are formed does not occur.
  • the rubber-modified thermoplastic resin (A) has a high rubber component content, the blending thereof even in a small amount results in an improvement in impact resistance and mechanical strength, so that various kinds of ABS resins can be easily prepared by selecting among many kinds of AB resins suitably. A lot of kinds of ABS resins can be further prepared, since amounts and kinds of additives and the like are possible to be widely varied in their use.
  • thermoplastic resins as AS resins are excellent in productivity and less expensive
  • the rubber-modified thermoplastic resin (A) of this invention can be blended therewith to mass-produce inexpensive ABS resins with an excellent productivity.
  • thermoplastic resin (A), the thermoplastic resin (B) and the additives shown in Table 2 were mixed in the amounts shown in Table 2 by means of a Henschel mixer and the mixture obtained was extruded from an extruder in which the cylinder set temperature was 200°C to obtain pellets.
  • Tensile strength and elongation were measured according to ASTM D638. Test specimen: ASTM type I Length: 21.6 cm Center width: 1.27 cm Thickness: 0.32 cm Speed of testing: 5.0 cm/min The tensile strength TS (kgf/cm 2 ) and elongation E (%) of each test specimen were calculated.
  • the flexural strength was measured according to ASTM D790. Test specimen: Length: 10.0 cm Width: 2.5 cm Thickness: 0.32 cm Rate of crosshead motion: 1.5 cm/min.
  • the flexural strength FS (kgf/cm 2 ) and flexural modulus FM (kgf/cm 2 ) of each test specimen were calculated.
  • ABS-4 The same procedure as in ABS-3 was repeated, except that t-butyl peroxyisopropyl carbonate was substituted for the cumene hydroperoxide to obtain ABS-4 as shown in Table 1.
  • AS-1 A copolymer of 75% of styrene and 25% of acrylonitrile having [ ⁇ ] (intrinsic viscosity of methyl ethyl ketone-soluble matter) of 0.4 dl/g as measured in methyl ethyl ketone at 30°C.
  • AS-2 A copolymer of 75% of styrene and 25% of acrylonitrile having [ ⁇ ] of 0.6 dl/g as measured in methyl ethyl ketone at 30°C.
  • AS-3 A copolymer of 70% of styrene and 30% of acrylonitrile having [ ⁇ ] of 0.7 dl/g as measured in methyl ethyl ketone at 30°C.
  • Examples 1 to 9 are thermoplastic resins in which a rubber-modified thermoplastic resin having a Q value falling within the scope of this invention was used.
  • Comparative Examples 1 and 3 are thermoplastic resins in which a rubber-modified thermoplastic resin having a Q value outside the scope of this invention was used.
  • ABS-9 was produced in the same manner as ABS-1 was; ABS-10 and ABS-12 were produced in the same manner as ABS-9 and ABS-11 were produced, respectively, except that t-butyl peroxyisopropyl carbonate was substituted for the cumene hydroperoxide.
  • ABS-11, ABS-13, ABS-14 and ABS-15 the same compounding recipe as in ABS-9 was used, except that the amounts of rubber, t-dodecylmercaptan and initiator were varied as shown in Table 3, and the other conditions were the same as in ABS-1.
  • Examples 10 to 18 are thermoplastic resin compositions in which a rubber-modified thermoplastic resin falling with the scope of this invention was used.
  • Examples 1 to 3 and 14 and 15 are excellent in gloss, impact resistance and fish eyes and also improved in mechanical strength.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Graft Or Block Polymers (AREA)
EP96300026A 1995-01-13 1996-01-03 Gummi-modifiziertes, thermoplastisches Harz und dieses enthaltende Zusammensetzung Expired - Lifetime EP0721962B1 (de)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
JP20934/95 1995-01-13
JP2093495 1995-01-13
JP02093495A JP3216466B2 (ja) 1995-01-13 1995-01-13 ゴム変性熱可塑性樹脂およびその組成物
JP148219/95 1995-05-23
JP14821995A JP3235411B2 (ja) 1995-05-23 1995-05-23 ゴム変性熱可塑性樹脂およびその組成物
JP14821995 1995-05-23

Publications (3)

Publication Number Publication Date
EP0721962A2 true EP0721962A2 (de) 1996-07-17
EP0721962A3 EP0721962A3 (de) 1997-06-18
EP0721962B1 EP0721962B1 (de) 2000-05-03

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EP96300026A Expired - Lifetime EP0721962B1 (de) 1995-01-13 1996-01-03 Gummi-modifiziertes, thermoplastisches Harz und dieses enthaltende Zusammensetzung

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Country Link
US (1) US5635565A (de)
EP (1) EP0721962B1 (de)
KR (1) KR100392314B1 (de)
DE (1) DE69607991T2 (de)

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EP1031609A1 (de) * 1999-02-26 2000-08-30 Techno Polymer Co., Ltd. Thermoplastische Gummizusammensetzung mit hervorragender Verschleissresistenz
EP2202273A1 (de) * 2008-12-29 2010-06-30 Cheil Industries Inc. Thermoplastisches Harz mit ausgezeichneter Wärmebeständigkeit und Schlagfestigkeit und dessen Herstellungsverfahren
EP2204415A1 (de) * 2008-12-29 2010-07-07 Cheil Industries Inc. Thermoplastisches Harz mit geringem Glanz und ausgezeichneter Wärmbeständigkeit und Stoßfestigkeit und dessen Herstellungsverfahren
US9365671B2 (en) 2013-12-04 2016-06-14 Samsung Sdi Co., Ltd. Styrene-based copolymer and thermoplastic resin composition including the same
US9790362B2 (en) 2014-06-27 2017-10-17 Lotte Advanced Materials Co., Ltd. Thermoplastic resin composition and molded article made using the same
US9850333B2 (en) 2014-06-27 2017-12-26 Lotte Advanced Materials Co., Ltd. Copolymers and thermoplastic resin composition including the same
US9856371B2 (en) 2014-06-27 2018-01-02 Lotte Advanced Materials Co., Ltd. Thermoplastic resin composition and low-gloss molded article made therefrom
US9862822B2 (en) 2014-11-18 2018-01-09 Lotte Advanced Materials Co., Ltd. Thermoplastic resin composition and molded article made using the same
US9902850B2 (en) 2014-06-26 2018-02-27 Lotte Advanced Materials Co., Ltd. Thermoplastic resin composition

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KR20030009856A (ko) * 2001-07-24 2003-02-05 주식회사 엘지화학 내충격성이 우수한 아크릴로니트릴-부타디엔-스티렌열가소성 수지의 제조방법
KR100933103B1 (ko) * 2002-11-21 2009-12-21 테크노 폴리머 가부시키가이샤 열가소성 수지 조성물, 차량 외장용 성형품용 열가소성수지 조성물, 차량 외장용 성형품 및 차량 외장용 성형품의제조 방법
KR100708995B1 (ko) * 2005-05-26 2007-04-18 주식회사 엘지화학 내충격성과 신율이 우수한 무광택 ａｂｓ 수지 조성물의제조방법 및 그로부터 수득되는 무광택 ａｂｓ 수지 조성물
EP2113002B1 (de) 2006-12-29 2013-07-17 Firestone Polymers, LLC Verfahren zur herstellung gummihaltiger polymerer zusammensetzungen und zusammensetzungen
KR100781965B1 (ko) * 2006-12-29 2007-12-06 제일모직주식회사 내충격성이 향상된 열가소성 수지 조성물
KR100875957B1 (ko) * 2007-12-28 2008-12-26 제일모직주식회사 압출 성형성이 향상된 내화학성 내충격성 열가소성 수지조성물
KR101150817B1 (ko) * 2008-12-15 2012-06-13 제일모직주식회사 유동성이 우수한 난연성 내충격 폴리스티렌 수지 조성물
KR101098281B1 (ko) * 2008-12-17 2011-12-23 제일모직주식회사 브롬화 디페닐에탄 혼합물, 그 제조방법 및 이를 이용한 수지 조성물
KR20100069878A (ko) * 2008-12-17 2010-06-25 제일모직주식회사 난연성 열가소성 수지 조성물
US8119720B2 (en) * 2008-12-29 2012-02-21 Cheil Industries Inc. Thermoplastic resin composition having improved flowability
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DE69607991D1 (de) 2000-06-08
EP0721962B1 (de) 2000-05-03
KR960029404A (ko) 1996-08-17
US5635565A (en) 1997-06-03
KR100392314B1 (ko) 2004-03-31
EP0721962A3 (de) 1997-06-18
DE69607991T2 (de) 2001-03-15

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